Variant report

Variant	nsv539601
Chromosome Location	chr8:50023423-50416049
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1884)
CpG islands
(count:183)
Chromatin interactive
region (count:112)
LncRNA
region (count:37)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1884 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:50189742-50189896	K562	blood:	n/a	n/a
2	ARID3A	chr8:50176389-50176820	K562	blood:	n/a	n/a
3	ARID3A	chr8:50142928-50143249	K562	blood:	n/a	n/a
4	ARID3A	chr8:50038776-50039400	K562	blood:	n/a	n/a
5	ARID3A	chr8:50042305-50042634	K562	blood:	n/a	n/a
6	ARID3A	chr8:50022835-50023624	K562	blood:	n/a	n/a
7	ARID3A	chr8:50037822-50038312	K562	blood:	n/a	n/a
8	ARID3A	chr8:50139129-50140149	K562	blood:	n/a	n/a
9	ARID3A	chr8:50137796-50138000	K562	blood:	n/a	n/a
10	ARID3A	chr8:50045458-50045469	K562	blood:	n/a	n/a
11	ARID3A	chr8:50142326-50142343	K562	blood:	n/a	n/a
12	ARID3A	chr8:50163861-50164727	K562	blood:	n/a	n/a
13	ARID3A	chr8:50033978-50034353	K562	blood:	n/a	n/a
14	ATF1	chr8:50119038-50119092	K562	blood:	n/a	n/a
15	ATF1	chr8:50204080-50204452	K562	blood:	n/a	n/a
16	ATF1	chr8:50213509-50213949	K562	blood:	n/a	n/a
17	ATF1	chr8:50042268-50042716	K562	blood:	n/a	n/a
18	ATF1	chr8:50043141-50043408	K562	blood:	n/a	n/a
19	ATF1	chr8:50139582-50140080	K562	blood:	n/a	n/a
20	ATF1	chr8:50146602-50146783	K562	blood:	n/a	n/a
21	ATF1	chr8:50129384-50129937	K562	blood:	n/a	n/a
22	ATF1	chr8:50164658-50164824	K562	blood:	n/a	n/a
23	ATF1	chr8:50176434-50176846	K562	blood:	n/a	n/a
24	ATF1	chr8:50141709-50141977	K562	blood:	n/a	n/a
25	ATF1	chr8:50212341-50212528	K562	blood:	n/a	n/a
26	ATF2	chr8:50064675-50065110	GM12878	blood:	n/a	n/a
27	ATF2	chr8:50135529-50136160	GM12878	blood:	n/a	n/a
28	ATF2	chr8:50063437-50063916	GM12878	blood:	n/a	n/a
29	ATF2	chr8:50211599-50211898	GM12878	blood:	n/a	n/a
30	ATF2	chr8:50164032-50164513	GM12878	blood:	n/a	n/a
31	ATF2	chr8:50135514-50136034	GM12878	blood:	n/a	n/a
32	ATF2	chr8:50063467-50063855	GM12878	blood:	n/a	n/a
33	ATF2	chr8:50064665-50065098	GM12878	blood:	n/a	n/a
34	ATF2	chr8:50164138-50164888	GM12878	blood:	n/a	n/a
35	ATF3	chr8:50042276-50042621	K562	blood:	n/a	chr8:50042553-50042561 chr8:50042553-50042563 chr8:50042549-50042564 chr8:50042551-50042564
36	BACH1	chr8:50039590-50039608	K562	blood:	n/a	n/a
37	BACH1	chr8:50033867-50033912	K562	blood:	n/a	n/a
38	BATF	chr8:50209651-50209963	GM12878	blood:	n/a	chr8:50209768-50209779
39	BATF	chr8:50084554-50084785	GM12878	blood:	n/a	n/a
40	BATF	chr8:50211556-50211991	GM12878	blood:	n/a	chr8:50211805-50211816
41	BATF	chr8:50164094-50164475	GM12878	blood:	n/a	n/a
42	BATF	chr8:50211604-50211957	GM12878	blood:	n/a	chr8:50211805-50211816
43	BATF	chr8:50279332-50279551	GM12878	blood:	n/a	n/a
44	BATF	chr8:50135732-50136065	GM12878	blood:	n/a	n/a
45	BATF	chr8:50064660-50065058	GM12878	blood:	n/a	n/a
46	BATF	chr8:50373415-50373752	GM12878	blood:	n/a	chr8:50373651-50373661 chr8:50373647-50373657
47	BATF	chr8:50284873-50285140	GM12878	blood:	n/a	n/a
48	BATF	chr8:50064654-50065062	GM12878	blood:	n/a	n/a
49	BATF	chr8:50135514-50135715	GM12878	blood:	n/a	n/a
50	BCL11A	chr8:50164150-50164454	GM12878	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:50314174-50314224	AG04449	skin:	fetal
2	chr8:50220067-50220117	HCPEpiC	choroid plexus:	n/a
3	chr8:50220067-50220117	NH-A	brain:	n/a
4	chr8:50213812-50213862	H1-hESC	embryonic stem cell:	embryo
5	chr8:50213812-50213862	CMK	blood:	n/a
6	chr8:50314174-50314224	AoSMC	blood vessel:	n/a
7	chr8:50314174-50314224	HCPEpiC	choroid plexus:	n/a
8	chr8:50213812-50213862	HEK293	kidney:	embryo
9	chr8:50213812-50213862	HAEpiC	amniotic membrane:	n/a
10	chr8:50213812-50213862	HCPEpiC	choroid plexus:	n/a
11	chr8:50220067-50220117	Caco-2	colon:	n/a
12	chr8:50314174-50314224	RPTEC	kidney:	n/a
13	chr8:50314174-50314224	HUVEC	blood vessel:	n/a
14	chr8:50220067-50220117	U87	brain:	n/a
15	chr8:50213812-50213862	GM19239	blood:	n/a
16	chr8:50213812-50213862	Caco-2	colon:	n/a
17	chr8:50314174-50314224	GM12891	blood:	n/a
18	chr8:50220067-50220117	K562	blood:	n/a
19	chr8:50213812-50213862	U87	brain:	n/a
20	chr8:50314174-50314224	NHDF-neo	bronchial:	n/a
21	chr8:50220067-50220117	Hepatocyte	liver:	n/a
22	chr8:50220067-50220117	PFSK-1	brain:	n/a
23	chr8:50220067-50220117	GM12891	blood:	n/a
24	chr8:50213812-50213862	ECC-1	luminal epithelium:	n/a
25	chr8:50213812-50213862	AG04450	lung:	fetal
26	chr8:50213812-50213862	HCT-116	colon:	n/a
27	chr8:50213812-50213862	RPTEC	kidney:	n/a
28	chr8:50314174-50314224	T-47D	breast:	n/a
29	chr8:50213812-50213862	A549	lung:	n/a
30	chr8:50314174-50314224	Hepatocyte	liver:	n/a
31	chr8:50220067-50220117	A549	lung:	n/a
32	chr8:50213812-50213862	IMR90	lung:	fetal
33	chr8:50213812-50213862	SKMC	muscle:	n/a
34	chr8:50314174-50314224	HL-60	blood:	n/a
35	chr8:50314174-50314224	GM12892	blood:	n/a
36	chr8:50314174-50314224	GM12878	blood:	n/a
37	chr8:50314174-50314224	MCF10A-Er-Src	breast:	n/a
38	chr8:50220067-50220117	NT2-D1	testis:	n/a
39	chr8:50314174-50314224	SK-N-SH_RA	brain:	n/a
40	chr8:50220067-50220117	GM12878	blood:	n/a
41	chr8:50314174-50314224	SK-N-MC	brain:	n/a
42	chr8:50314174-50314224	AG10803	skin:	n/a
43	chr8:50213812-50213862	SK-N-SH_RA	brain:	n/a
44	chr8:50220067-50220117	PANC-1	pancreas:	n/a
45	chr8:50314174-50314224	HAEpiC	amniotic membrane:	n/a
46	chr8:50213812-50213862	Hela-S3	cervix:	n/a
47	chr8:50220067-50220117	SK-N-MC	brain:	n/a
48	chr8:50220067-50220117	HUVEC	blood vessel:	n/a
49	chr8:50220067-50220117	ProgFib	skin:	n/a
50	chr8:50213812-50213862	SK-N-MC	brain:	n/a

(count:112 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:50151168..50153815-chr8:50156389..50158131,2	K562	blood:
2	chr8:50189228..50191927-chr8:50203055..50205664,2	K562	blood:
3	chr8:50032130..50034951-chr8:50036647..50039869,3	K562	blood:
4	chr8:50031366..50035096-chr8:50036647..50040169,3	K562	blood:
5	chr8:50189228..50191927-chr8:50203055..50205664,2	K562	blood:
6	chr8:50130806..50133714-chr8:50138525..50141483,2	K562	blood:
7	chr8:50157596..50161511-chr8:50162518..50165588,4	K562	blood:
8	chr8:50306965..50309491-chr8:50313061..50314583,2	K562	blood:
9	chr8:50223069..50226256-chr8:50227030..50231187,6	K562	blood:
10	chr8:50122009..50123670-chr8:50128301..50129864,2	K562	blood:
11	chr8:50157489..50159096-chr8:50164088..50165590,2	K562	blood:
12	chr8:50286271..50288690-chr8:50292901..50294552,2	K562	blood:
13	chr8:50224322..50226256-chr8:50228266..50231187,2	K562	blood:
14	chr8:50157596..50161511-chr8:50162518..50165588,4	K562	blood:
15	chr8:50083760..50086501-chr8:50089833..50092673,4	K562	blood:
16	chr8:50031366..50035096-chr8:50036647..50040169,3	K562	blood:
17	chr8:50114787..50117721-chr8:50120524..50123676,3	K562	blood:
18	chr8:50174406..50177036-chr8:50205443..50207064,2	K562	blood:
19	chr8:50029029..50031186-chr8:50035515..50038037,2	K562	blood:
20	chr8:50306312..50308605-chr8:50313083..50315723,3	K562	blood:
21	chr8:50288741..50291361-chr8:50315909..50318142,2	K562	blood:
22	chr8:50187361..50189118-chr8:50190967..50193350,2	K562	blood:
23	chr8:50306965..50309491-chr8:50313061..50314583,2	K562	blood:
24	chr8:50198141..50200837-chr8:50202344..50203937,2	K562	blood:
25	chr8:50201423..50203830-chr8:50212097..50214084,2	K562	blood:
26	chr8:50201423..50204477-chr8:50211622..50215340,4	K562	blood:
27	chr8:50174406..50177036-chr8:50205443..50207064,2	K562	blood:
28	chr8:49978220..49980915-chr8:50057645..50059549,2	K562	blood:
29	chr8:49959412..49962230-chr8:50108460..50111062,2	K562	blood:
30	chr8:50023484..50026392-chr8:50032948..50035396,2	K562	blood:
31	chr8:50052841..50054803-chr8:50061122..50063671,2	K562	blood:
32	chr8:50207112..50210089-chr8:50216692..50218806,2	K562	blood:
33	chr8:50052841..50054803-chr8:50061122..50063671,2	K562	blood:
34	chr8:50220433..50222102-chr8:50312150..50314977,2	K562	blood:
35	chr8:50256870..50259516-chr8:50263115..50264722,2	K562	blood:
36	chr8:50142308..50144994-chr8:50148031..50149920,2	K562	blood:
37	chr8:50154056..50156142-chr8:50160235..50163146,3	K562	blood:
38	chr8:50036565..50039449-chr8:50040680..50044061,3	K562	blood:
39	chr8:50220131..50222425-chr8:50223280..50225514,2	K562	blood:
40	chr8:50307157..50309606-chr8:50310313..50312486,2	K562	blood:
41	chr8:50169460..50172760-chr8:50198302..50201832,3	K562	blood:
42	chr8:50056870..50059672-chr8:50062118..50064411,2	K562	blood:
43	chr8:50037357..50040620-chr8:50040803..50044061,4	K562	blood:
44	chr8:50158291..50160893-chr8:50161385..50163707,3	K562	blood:
45	chr8:50154600..50156142-chr8:50160235..50163146,2	K562	blood:
46	chr8:50207112..50210089-chr8:50216692..50218806,2	K562	blood:
47	chr8:50224322..50226256-chr8:50228266..50231187,2	K562	blood:
48	chr8:50256870..50259516-chr8:50263115..50264722,2	K562	blood:
49	chr8:50032130..50034951-chr8:50036647..50039869,3	K562	blood:
50	chr8:50151168..50153815-chr8:50156389..50158131,2	K562	blood:

(count:37 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8orf22-12	chr8:50243331-50243643	l_3592_chr8:50243194-50268365_ovary
2	lnc-RP11-738G5.2.1-4	chr8:50313617-50313650	NONHSAT126516
3	lnc-C8orf22-2	chr8:50081241-50081368	ENSG00000253474
4	lnc-C8orf22-12	chr8:50243195-50243330	l_3592_chr8:50243194-50268365_ovary
5	lnc-C8orf22-12	chr8:50243796-50243921	l_3592_chr8:50243194-50268365_ovary
6	lnc-C8orf22-2	chr8:50141117-50141484	ENSG00000253474
7	lnc-SNAI2-1	chr8:50047181-50047788	NONHSAT126505
8	lnc-RP11-738G5.2.1-5	chr8:50265189-50265403	NONHSAT126515
9	lnc-C8orf22-10	chr8:50242769-50243106	NONHSAT126514
10	lnc-C8orf22-2	chr8:50105666-50105812	XLOC_006793
11	lnc-C8orf22-2	chr8:50141116-50142388	NONHSAT126506
12	lnc-C8orf22-2	chr8:50118940-50119026	NONHSAT126506
13	lnc-C8orf22-2	chr8:50137496-50137609	NONHSAT126506
14	lnc-C8orf22-2	chr8:50137497-50137609	ENSG00000253474
15	lnc-C8orf22-2	chr8:50081098-50081368	ENSG00000253474
16	lnc-C8orf22-2	chr8:50140699-50140944	XLOC_006794
17	lnc-C8orf22-2	chr8:50103993-50107149	NONHSAT126506
18	lnc-C8orf22-12	chr8:50268219-50268365	l_3592_chr8:50243194-50268365_ovary
19	lnc-C8orf22-2	chr8:50080642-50080861	XLOC_006793
20	lnc-C8orf22-2	chr8:50140699-50140779	ENSG00000253474
21	lnc-C8orf22-2	chr8:50081243-50081368	XLOC_006793
22	lnc-C8orf22-2	chr8:50141117-50142346	XLOC_006794
23	lnc-RP11-738G5.2.1-4	chr8:50307783-50308267	NONHSAT126516
24	lnc-C8orf22-2	chr8:50080642-50081090	XLOC_006793
25	lnc-C8orf22-2	chr8:50081243-50081368	XLOC_006793
26	lnc-C8orf22-2	chr8:50140698-50140779	NONHSAT126506
27	lnc-C8orf22-2	chr8:50137500-50137588	ENSG00000253474
28	lnc-RP11-738G5.2.1-6	chr8:50209735-50210341	ucscGeneNc_uc003xqr_2
29	lnc-C8orf22-2	chr8:50137497-50137609	XLOC_006794
30	lnc-C8orf22-2	chr8:50140699-50140779	XLOC_006794
31	lnc-C8orf22-2	chr8:50105666-50105812	XLOC_006793
32	lnc-C8orf22-2	chr8:50137497-50137609	XLOC_006794
33	lnc-C8orf22-2	chr8:50105666-50105754	ENSG00000253474
34	lnc-C8orf22-2	chr8:50080641-50081407	NONHSAT126506
35	lnc-RP11-738G5.2.1-1	chr8:50409322-50409534	ENSG00000253380
36	lnc-RP11-738G5.2.1-4	chr8:50312748-50312854	NONHSAT126516
37	lnc-RP11-738G5.2.1-1	chr8:50409334-50409534	XLOC_007081

No data

Variant related genes	Relation type
RFPL4AP7	TF binding region
RN7SKP294	TF binding region
ENSG00000253474	TF binding region
RFPL4AP7	CpG island
RN7SKP294	CpG island
ENSG00000253474	CpG island
ENSG00000253474	chromatin interactions

Extended variants
information (count: 6927 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:6927 , 50 per page) page: 1 2 3 4 5 6 7 ... 139

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534315443	chr8:50023518-50023519	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs547278404	chr8:50023535-50023536	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs571369019	chr8:50023549-50023550	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs192625358	chr8:50023571-50023572	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs341817	chr8:50023600-50023601	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs183915488	chr8:50023630-50023631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575719305	chr8:50023635-50023636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539362635	chr8:50023753-50023754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs188242299	chr8:50023774-50023775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs12548464	chr8:50023867-50023868	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs115663850	chr8:50023874-50023875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs528095146	chr8:50023878-50023879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs192684289	chr8:50023892-50023893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111325534	chr8:50023949-50023950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564886469	chr8:50023990-50023991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs184921469	chr8:50024034-50024035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs10101461	chr8:50024039-50024040	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs147247129	chr8:50024083-50024084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs563501322	chr8:50024136-50024137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113571530	chr8:50024141-50024142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549300856	chr8:50024145-50024146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs116574841	chr8:50024164-50024165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs77778531	chr8:50024216-50024217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190224099	chr8:50024228-50024229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571227566	chr8:50024260-50024261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs145202096	chr8:50024310-50024311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375231871	chr8:50024311-50024312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs61486927	chr8:50024315-50024316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs117100725	chr8:50024334-50024335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs557069409	chr8:50024340-50024341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10101898	chr8:50024358-50024359	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs529866374	chr8:50024397-50024398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546601977	chr8:50024424-50024425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs536433850	chr8:50024476-50024477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs555287334	chr8:50024516-50024517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs575812674	chr8:50024531-50024532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs540493393	chr8:50024532-50024533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs558552817	chr8:50024593-50024594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs116446614	chr8:50024659-50024660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs544336145	chr8:50024708-50024709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs144737787	chr8:50024740-50024741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs182040274	chr8:50024741-50024742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs542460296	chr8:50024791-50024792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs186669327	chr8:50024805-50024806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545955934	chr8:50024818-50024819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs546888834	chr8:50024835-50024836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs12056729	chr8:50024894-50024895	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs376423163	chr8:50024926-50024927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs10504073	chr8:50024944-50024945	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
50	rs568855252	chr8:50024960-50024961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Ovarian cancer	22174824	CNVD

Chromatin state (count:426 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:50019200-50023600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr8:50020600-50025800	Weak transcription	Fetal Lung	lung
3	chr8:50022200-50023600	Enhancers	NHEK	skin
4	chr8:50022600-50023600	Enhancers	K562	blood
5	chr8:50022800-50023600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
6	chr8:50022800-50023600	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr8:50023000-50023600	Enhancers	Stomach Mucosa	stomach
8	chr8:50023400-50023600	Enhancers	Gastric	stomach
9	chr8:50023400-50026200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr8:50023600-50024400	Weak transcription	Stomach Mucosa	stomach
11	chr8:50023600-50025200	Weak transcription	K562	blood
12	chr8:50024400-50024800	Enhancers	Stomach Mucosa	stomach
13	chr8:50024800-50025000	Weak transcription	Stomach Mucosa	stomach
14	chr8:50025000-50025400	Enhancers	Stomach Mucosa	stomach
15	chr8:50025200-50025600	Enhancers	K562	blood
16	chr8:50025600-50028400	Weak transcription	K562	blood
17	chr8:50025800-50028400	Enhancers	Fetal Lung	lung
18	chr8:50026000-50026200	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr8:50026200-50028800	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr8:50028400-50029000	Enhancers	K562	blood
21	chr8:50034000-50034200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr8:50037600-50038000	Enhancers	K562	blood
23	chr8:50038000-50038400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr8:50038000-50038400	Flanking Active TSS	K562	blood
25	chr8:50038400-50039000	Active TSS	K562	blood
26	chr8:50039000-50039400	Flanking Active TSS	K562	blood
27	chr8:50039400-50039800	Enhancers	K562	blood
28	chr8:50039800-50040200	Flanking Active TSS	K562	blood
29	chr8:50040200-50040400	Active TSS	K562	blood
30	chr8:50040400-50041400	Weak transcription	K562	blood
31	chr8:50041400-50042800	Enhancers	K562	blood
32	chr8:50042800-50043000	Flanking Active TSS	K562	blood
33	chr8:50043000-50043200	Enhancers	K562	blood
34	chr8:50043200-50043400	Flanking Active TSS	K562	blood
35	chr8:50043400-50044200	Enhancers	K562	blood
36	chr8:50044200-50044600	Flanking Active TSS	K562	blood
37	chr8:50044600-50046000	Enhancers	K562	blood
38	chr8:50063200-50064600	Enhancers	GM12878-XiMat	blood
39	chr8:50064200-50065200	Enhancers	K562	blood
40	chr8:50064600-50065000	Flanking Active TSS	GM12878-XiMat	blood
41	chr8:50065000-50066000	Enhancers	GM12878-XiMat	blood
42	chr8:50066000-50069000	Weak transcription	GM12878-XiMat	blood
43	chr8:50069000-50069200	ZNF genes & repeats	GM12878-XiMat	blood
44	chr8:50069000-50069600	Active TSS	Fetal Lung	lung
45	chr8:50069600-50069800	Enhancers	Fetal Lung	lung
46	chr8:50075200-50076400	Enhancers	Stomach Mucosa	stomach
47	chr8:50076400-50079200	Weak transcription	Stomach Mucosa	stomach
48	chr8:50079200-50080800	Enhancers	Stomach Mucosa	stomach
49	chr8:50079400-50080600	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr8:50080000-50081000	Enhancers	NHEK	skin

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